Does DOCUSATE Cause Wrong patient received product? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Wrong patient received product have been filed in association with DOCUSATE (SENNA-S). This represents 0.9% of all adverse event reports for DOCUSATE.
23
Reports of Wrong patient received product with DOCUSATE
0.9%
of all DOCUSATE reports
21
Deaths
0
Hospitalizations
How Dangerous Is Wrong patient received product From DOCUSATE?
Of the 23 reports, 21 (91.3%) resulted in death.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOCUSATE. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does DOCUSATE Cause?
Somnolence (514)
Gastrooesophageal reflux disease (419)
Pneumonia aspiration (341)
Coma (337)
Constipation (329)
Drug ineffective (288)
Dyspnoea (277)
Off label use (236)
Vomiting (207)
Pain (195)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which DOCUSATE Alternatives Have Lower Wrong patient received product Risk?
DOCUSATE vs DOCUSATE\SENNOSIDES
DOCUSATE vs DOCUSATE\SENNOSIDES A AND B
DOCUSATE vs DOFETILIDE
DOCUSATE vs DOLUTEGRAVIR
DOCUSATE vs DOLUTEGRAVIR\LAMIVUDINE